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Mendeleev Communications, 2019, Volume 29, Issue 6, Pages 680–682
DOI: https://doi.org/10.1016/j.mencom.2019.11.026
(Mi mendc1629)
 

Communications

Synthesis of N-acetyllactosamine based branched hexasaccharide

I. M. Ryzhov, M. S. Savchenko, G. V. Pazynina, S. V. Tsygankova, I. S. Popova, T. V. Tyrtysh, N. V. Bovin

M.M. Shemyakin–Yu.A. Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Abstract: The protected spacer-armed branched tri-N-acetyllactosamine has been synthesized as a building block for the synthesis of biantennary ABH blood group antigens. The key synthetic step is the simultaneous glycosylation of the 3′- and 6′-OH groups of an N-acetyllactosamine glycosyl acceptor by N-Troc-lactosamine trichloroacetimidate.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (633.2 Kb)


Citation: I. M. Ryzhov, M. S. Savchenko, G. V. Pazynina, S. V. Tsygankova, I. S. Popova, T. V. Tyrtysh, N. V. Bovin, “Synthesis of N-acetyllactosamine based branched hexasaccharide”, Mendeleev Commun., 29:6 (2019), 680–682
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